Puchetti V, Modena S, Abrescia F, Canton C, Carolo F
Chir Ital. 1976 Dec;28(6):632-64.
Thirteen cases of congenital anomalies of the bile passages are described, as observed in the Verona Surgical Clinic during the period 1970-75, out of a total of 908 operations on the biliary passages and hence with a frequency of about 1.6%. They consisted of one case each of agenesis of the gall-bladder, septal gall-bladder, clepsydra gall-bladder, Hartmann's sac, diverticulum of the gall-bladder, outlet of the right hepatic in gall-bladder, outlet of cystic duct in third duodenal portion, accessory cholecystobiliary ducts, three cases of outlet of cystic duct in right hepatic duct, and two cases of common choledocho-wirsunghian canal. After a brief description of the individual types of anomaly, the main data in the relevant literature are considered, with a review of the semeiological and therapeutic aspects of the most frequent anomalies.
本文描述了1970年至1975年期间在维罗纳外科诊所观察到的13例先天性胆道异常病例,这些病例出自908例胆道手术,发生率约为1.6%。其中包括胆囊缺如、间隔胆囊、壶腹胆囊、哈特曼囊、胆囊憩室、右肝管开口于胆囊、胆囊管开口于十二指肠第三部、副胆囊胆管各1例,胆囊管开口于右肝管3例,胆总管-胰管共同通道2例。在对各类型异常进行简要描述后,考虑了相关文献中的主要数据,并对最常见异常的症状学和治疗方面进行了综述。